|
Dermatopathology
Case 106
Desmoplastic Spitz nevus (DSN) is
a rare variant of spitzoid tumours characterized by dermal proliferation
of large epitheliod and/or fusiform melanocytes within a
desmoplastic stroma, comprising thick,
eosinophilic collagen bundles.
Desmoplastic Spitz naevus (DSN) was first
described by Reed et al. in 1975
It has clinical and histopathological
features that are difficult to differentiate from dermatofibroma and
desmoplastic malignant melanoma (DMM), which requires aggressive therapy
for cure.
Images of
Desmoplastic
Spitz Nevus
It occurs most frequently in young
adults and children
It is usually a red-brown papule or
nodule, located on the extremities. However, lesions located on the
abdomen, head and neck region and a case with multiple lesions have been
reported
Differential diagnosis:
Spitz naevus: It is
differentiated from classical variants of Spitz naevi by lack of
dermoepidermal activity, absence of Kamino bodies, increased dermal
collagen and presence of ganglion-like epithelioid cells.
Dermatofibroma: The DSN can be
mistaken for dermatofibroma due to similar location and clinical
appearance. It can be differentiated precisely from dermatofibroma with
the presence of melanocytes and the positive immunohistochemical
staining of the cells with S-100 protein and antibody HMB-45.
Desmoplastic malignant melanoma:
From a histopathological point of view, symmetry, circumscription,
melanocytic maturation and involvement of adnexal structure are
significantly more frequent in desmoplastic
Spitz nevi. The presence of melanocytic
junctional nests associated with discohesive cells, variations in size
and shape of the nests, lentiginous melanocytic proliferation, actinic
elastosis, pagetoid spread, dermal mitosis, perineural involvement and
brisk inflammatory infiltrate are significantly more frequent in
desmoplastic melanoma. No significant
difference is found concerning epidermal hyperplasia, presence of Kamino
bodies or moderate inflammatory infiltrate. |